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FDA 510(k)

PNEUMATIC DORSIFLEXOR

K-Number: K890200 · 1989-02-03

ApplicantMedical Flotation Systems, Inc.
Decision Date1989-02-03
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PNEUMATIC DORSIFLEXOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Flotation Systems, Inc.. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K890200. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PNEUMATIC DORSIFLEXOR?

PNEUMATIC DORSIFLEXOR is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Medical Flotation Systems, Inc.. The 510(k) number is K890200.

When did PNEUMATIC DORSIFLEXOR receive FDA 510(k) clearance?

PNEUMATIC DORSIFLEXOR received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890200.

Who is the listed applicant for PNEUMATIC DORSIFLEXOR?

The FDA 510(k) record lists Medical Flotation Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PNEUMATIC DORSIFLEXOR?

The FDA product code for PNEUMATIC DORSIFLEXOR is BXB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Flotation Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K893801M.F.S. LOW AIR LOSS PULSATING BEDK884907BUMPY MEDICAL MASSAGE MATK884908ULTRAFLOTATION MEDICAL WHEELCHAIRK882607ULTRAFLOTATION BED

Related Devices (Code: BXB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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